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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491636Generated: October 31, 2026

HCID 18953543, compound → 4-(1H-imidazol-1-yl)pyridin-3-amine

https://huagongshe.com/reaction/1491636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18953543HCID 18953543—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product4-(1H-imidazol-1-yl)pyridin-3-amineHCID 1895354891.9%

Reaction Steps

4-(1-Imidazolyl)-3-nitropyridine (2.10 g, 11.0 mmol) was dissolved in 20 ml of ethanol. After the atmosphere was replaced with nitrogen, 0.25 g of 10% palladium-carbon was added thereto. After the atmosphere was replaced with hydrogen, hydrogen addition was conducted with stirring at room temperature for 3 days. Palladium-carbon was removed by filtration and the filtered cake was washed with ethanol. The filtrate and the washings were combined and then concentrated. The residue was purified by silica gel column chromatography [eluent: dichloromethane:methanol=8:1-6:1 (v/v)] to obtain 1.62 g of a light brown solid (yield: 91.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371086
Source datasetuspto-grants-1994_12
ORD IDord-c9dfc296919e4e01a85f1da252008546
Source noteuspto-grants-1994_12